CRUSH Alerts 2.0 - New Fortune 1000 Product Recall Announcements

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Trigger > Product Recall NEW

Generated using NewsCore by SalesQuest - Custom Classified Content

Recalls: Costco, Walmart, Big Lots, Ross
Monday February 6th 2012 09:53:00 PM

Six companies are recalling various products sold at several retailers including Costco, Walmart, Big Lots, Ross Dress For Less, Dd's Discounts, The Container Store and West Elm, according to recent reports from the U.S. Consumer Product Safety...

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North American Rescue, LLC Announces A Follow-Up to the Recall of Crickit Convenience Kits Because of Possible Health Risk Related to Nationwide Recall of Triad Povidone Iodine Prep Pads
Monday February 6th 2012 04:32:00 PM

Under the direction of the FDA, North American Rescue, LLC (NAR) today announces the market recall of the NAR Surgical Crichothyroidotomy Kit or Crickit, due to potential contamination of the povidone iodine prep pads, manufactured by Triad Group. This recall is a follow up to the recall initiated on May 5, 2011. North American Rescue, LLC has successfully contacted 97% of our customers and requested they contact our customer service department for return instructions.

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Healthy People Co. Dietary Supplements: Recall - Undeclared Drug Ingredient
Monday February 6th 2012 10:00:00 AM

Recalled products pose significant risk to patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke.

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Jammy Sammy PB & J bars recalled; no peanut warning on inner label
Monday February 6th 2012 07:23:06 AM

Revolution Foods, a company in the Nest Collective group of consumer products, has recalled Jammy Sammy Strawberry Jam & Peanut Butter Flavor Snack Size Sandwich Bars due to a mislabeled inner wrapper. Revolution Foods, a company in the Nest Collective group of consumer products, has recalled Jammy Sammy Strawberry Jam & Peanut Butter Flavor Snack Size Sandwich Bars due to a mislabeled inner wrapper.

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Bill Would Block FDA 510(k) Approval For Medical Devices Associated With Recalls
Sunday February 5th 2012 08:20:04 PM

Bernstein Liebhard reports on a newly introduced bill that would prevent medical device manufacturers from using the 510(k) process to receive FDA approval if they are predicated on previously recalled products.

(PRWeb February 05, 2012)

Read the full story at http://www.prweb.com/releases/vaginal-mesh-lawsuit/consumer-injury-lawyers/prweb9167102.htm

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January Recall Recap: Freezer Packs, High Chairs and Bike Trailers top the List
Sunday February 5th 2012 04:09:48 PM

The Consumer Product Safety Commission (CPSC) announced 25 recalls in January, including one expansion of a previously recalled bicycle. While that is slightly more than the 23 recalls we saw in December, it is still lower than we typically see...

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